Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26310 | A09 | 17077822 | G | A | upstream_gene_variant | MODIFIER | c.-283G>A| |
S1 S228 |
2 | BAA09g26310 | A09 | 17077833 | C | T | upstream_gene_variant | MODIFIER | c.-272C>T| |
S19 |
3 | BAA09g26310 | A09 | 17078146 | G | A | synonymous_variant | LOW | c.42G>A|p.Val14Val |
S280 |
4 | BAA09g26310 | A09 | 17078163 | C | T | missense_variant | MODERATE | c.59C>T|p.Ala20Val |
S136 |
5 | BAA09g26310 | A09 | 17079444 | C | T | intron_variant | MODIFIER | c.328-42C>T| |
S172 S217 |
6 | BAA09g26310 | A09 | 17079446 | G | A | intron_variant | MODIFIER | c.328-40G>A| |
S57 |
7 | BAA09g26310 | A09 | 17079984 | C | T | missense_variant | MODERATE | c.638C>T|p.Pro213Leu |
S277 |
8 | BAA09g26310 | A09 | 17080044 | G | A | intron_variant | MODIFIER | c.654-37G>A| |
S46 |
9 | BAA09g26310 | A09 | 17080527 | C | T | synonymous_variant | LOW | c.849C>T|p.Asp283Asp |
S231 |
10 | BAA09g26310 | A09 | 17081418 | C | T | intron_variant | MODIFIER | c.1201+32C>T| |
S62 |
11 | BAA09g26310 | A09 | 17081852 | C | T | intron_variant | MODIFIER | c.1412+131C>T| |
S19 |
12 | BAA09g26310 | A09 | 17082036 | C | T | intron_variant | MODIFIER | c.1413-111C>T| |
S128 |
13 | BAA09g26310 | A09 | 17085623 | G | C | downstream_gene_variant | MODIFIER | c.*1976G>C| |
S127 |
14 | BAA09g26310 | A09 | 17085656 | G | A | downstream_gene_variant | MODIFIER | c.*2009G>A| |
S271 |
15 | BAA09g26310 | A09 | 17085934 | C | T | downstream_gene_variant | MODIFIER | c.*2287C>T| |
S9 |
16 | BAA09g26310 | A09 | 17086316 | G | A | downstream_gene_variant | MODIFIER | c.*2669G>A| |
S110 |
17 | BAA09g26310 | A09 | 17087719 | C | T | downstream_gene_variant | MODIFIER | c.*4072C>T| |
S32 |
18 | BAA09g26310 | A09 | 17087747 | C | T | downstream_gene_variant | MODIFIER | c.*4100C>T| |
S159 S243 S299 |
19 | BAA09g26310 | A09 | 17088432 | G | A | downstream_gene_variant | MODIFIER | c.*4785G>A| |
S98 |